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[肿瘤坏死因子-α 诱导人脐静脉内皮细胞线粒体释放锰超氧化物歧化酶]

[Induction and release of manganese superoxide dismutase caused by tumor necrosis factor-alpha from mitochondria in human umbilical vein endothelial cells].

作者信息

Nakata T

机构信息

Department of Obstetrics and Gynecology, Asahikawa Medical College.

出版信息

Nihon Sanka Fujinka Gakkai Zasshi. 1995 Dec;47(12):1345-51.

PMID:8568353
Abstract

The effects of tumor necrosis factor-alpha (TNF-alpha) on cultured human umbilical vein endothelial cells (EC) and five cancer cell lines, A549, ME180, A2780, KURAMOCHI, and Hela, were compared. While A549, A2780, KURAMOCHI, and Hela cells were fairly resistant to the cytolytic effects of TNF-alpha, ME180 cells were sensitive. EC were also less sensitive to TNF-alpha than ME180 cells as judged by the viability of individual cells and by the release of lactate dehydrogenase (LDH) into the medium. Manganese superoxide dismutase (Mn-SOD) was markedly induced by these cytokines in EC and in A549 cells but not in ME180 cells. The levels of Mn-SOD in the conditioned medium of EC were dramatically increased after stimulation with cytokines, whereas those in ME180 and A549 cells were relatively low. The amount of Mn-SOD released appears to be comparable to that from cells lysed by other means. Immunoblot analysis of Mn-SOD in the medium showed that the molecular mass of the immunoreactive protein was the same as mitochondrial Mn-SOD, indicating that no proteolysis had occurred. These data suggest that in vivo the TNF-alpha produced by cancer cells may induce Mn-SOD in vascular endothelial cells, resulting in release of a relatively large amount of this protein into the serum.

摘要

比较了肿瘤坏死因子-α(TNF-α)对培养的人脐静脉内皮细胞(EC)以及5种癌细胞系A549、ME180、A2780、仓持和Hela的影响。虽然A549、A2780、仓持和Hela细胞对TNF-α的细胞溶解作用相当耐受,但ME180细胞敏感。根据单个细胞的活力以及乳酸脱氢酶(LDH)释放到培养基中的情况判断,EC对TNF-α的敏感性也低于ME180细胞。这些细胞因子在EC和A549细胞中可显著诱导锰超氧化物歧化酶(Mn-SOD),但在ME180细胞中则不然。用细胞因子刺激后,EC条件培养基中Mn-SOD的水平显著升高,而ME180和A549细胞中的水平相对较低。释放的Mn-SOD量似乎与通过其他方式裂解细胞释放的量相当。对培养基中Mn-SOD的免疫印迹分析表明,免疫反应性蛋白的分子量与线粒体Mn-SOD相同,这表明未发生蛋白水解。这些数据表明,在体内癌细胞产生的TNF-α可能诱导血管内皮细胞中的Mn-SOD,导致相对大量的该蛋白释放到血清中。

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